scholarly journals A Rare Case of Omphalocele, Exstrophy of Bladder, Imperforate Anus and Spinal Defect Complex with Genital Anomalies in a Term Neonate

2021 ◽  
Vol 18 (3) ◽  
Author(s):  
Deepali Ambike ◽  
Abhijeet Byale ◽  
Rijwana Sayyad ◽  
Vinit Rathod ◽  
Komal Bijarniya
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Term Neonate ◽  
Defect Complex

scholarly journals Complete Penoscrotal Transposition with Other Extragenital Anomalies in a Neonate Delivered at Term

2021 ◽  
Vol 2021 ◽  
pp. 1-4
Author(s):  
Ali Mahamudu Ayamba ◽  
Raymond Saa-Eru Maalman ◽  
Yaw Otchere Donkor ◽  
John Noah Anyorigiya
Keyword(s):  
Imperforate Anus ◽  
Rare Case ◽  
Term Neonate ◽  
Cardiac Malformation ◽  
Facial Deformity ◽  
Antenatal Services ◽  
Penoscrotal Transposition

A complete penoscrotal transposition (CPST) is a very uncommon congenital maldevelopment that is always associated with other abnormal body variations (malformations). We report a rare case of a term neonate delivered with CPST, which had a flaccid penis and an intact scrotum with unilateral limb and digital deformity, imperforate anus, cardiac malformation a facial deformity. Neonate died two hours after delivery. The foetal abnormality was not detected through routine antenatal services received by the mother.

scholarly journals A rare case of perineal hamartoma associated with cryptorchidism and imperforate anus: case report

2014 ◽  
Vol 12 (2) ◽  
pp. 234-236
Author(s):  
Kleiton Gabriel Ribeiro Yamaçake ◽  
Amilcar Martins Giron ◽  
Uenis Tannuri ◽  
Miguel Srougi
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Imperforate Anus ◽  
Rare Case ◽  
Coloanal Anastomosis ◽  
Histopathological Examination ◽  
Congenital Clubfoot ◽  
Anorectal Anomaly ◽  
Male Neonate ◽  
Nonpalpable Testis

A full-term male neonate with anorectal anomaly and external perineal anomalies was referred to our service. Physical examination showed an epithelized perineal mass with cutaneous orifices, which had urine fistulization, hipotrofic perineal musculature, bilateral congenital clubfoot, hipospadic urethra, criptorquidy bilateral with nonpalpable testis and imperforate anus. A colostomy was constructed immediately after birth. The child underwent excision of perineal mass, bilateral orchidopexy, Duplay neourethroplasty and coloanal anastomosis at 3 months of age. The histopathological examination of the perineal mass revealed a hamartoma.

Rectal adenocarcinoma following imperforate anus: A rare case report

2020 ◽  
pp. 252-254
Author(s):  
Sarah Khan ◽  
Hina Khan ◽  
Jan Agha ◽  
Khursheed Samo ◽  
Mujeeb Abbasi ◽  
...  
Keyword(s):  
Case Report ◽  
Imperforate Anus ◽  
Rare Case ◽  
Rectal Adenocarcinoma ◽  
Rare Case Report

scholarly journals A RARE CASE OF BIFID PENIS WITH IMPERFORATE ANUS

2014 ◽  
Vol 3 (48) ◽  
pp. 11614-11616
Author(s):  
Sharan Deshmukh ◽  
Shrikant S W ◽  
Sharangouda Patil ◽  
Harilal Naik M L
Keyword(s):  
Imperforate Anus ◽  
Rare Case

Currarino syndrome and spinal dysraphism

2014 ◽  
Vol 13 (6) ◽  
pp. 685-689 ◽  
Author(s):  
Matthew J. Kole ◽  
Jared S. Fridley ◽  
Andrew Jea ◽  
Robert J. Bollo
Keyword(s):  
Imperforate Anus ◽  
Congenital Anomalies ◽  
Rare Case ◽  
Spinal Dysraphism ◽  
Tethered Cord ◽  
Tethered Cord Syndrome ◽  
Presacral Mass ◽  
Occult Spinal Dysraphism ◽  
Spinal Lipoma ◽  
Currarino Syndrome

Currarino syndrome is a rare constellation of congenital anomalies characterized by the triad of sacral dysgenesis, presacral mass, and anorectal malformation. It is frequently associated with other congenital anomalies, often including occult spinal dysraphism. Mutations in the MNX1 gene are identified in the majority of cases. The authors report a rare case of Currarino syndrome in an infant with tethered cord syndrome and a dorsal lipomyelomeningocele continuous with a presacral intradural spinal lipoma, in addition to an imperforate anus and a scimitar sacrum. They review the literature to highlight patterns of occult spinal dysraphism in patients with Currarino syndrome and their relationship to tethered cord syndrome. Approximately 60% of the patients with Currarino syndrome reported in the literature have an occult spinal dysraphism. Published studies suggest that the risk of tethered cord syndrome may be higher among patients with a lipoma and lower among those with a teratoma or anterior meningocele.

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